A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv282n71



Internal ID6317902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103336601..103548497hg19UCSC Ensembl
chr1:103109189..103321085hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv871475, nsv871078, nsv870600, nsv870607, nsv871741
SamplesMS19634, MS15199, SP52094, MS18620, MS18978, MS20872
Known GenesCOL11A1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv282n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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